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NCT ID: NCT04110977 Recruiting - Clinical trials for Radiation Dermatitis

A Reminder App to Reduce Radiation Dermatitis Rates in Patients With Head-and-Neck Cancer

RAREST-02
Start date: October 10, 2020
Phase: N/A
Study type: Interventional

The goal of this randomized trial is to investigate whether the addition of a reminder app to standard care leads to a reduction of dermatitis and oral mucositis during radio(chemo)therapy for locally advanced squamous cell carcinoma of the head-and-neck (SCCHN). The primary endpoint is the rate of patients experiencing grade ≥2 radiation dermatitis at 60 Gy of radiotherapy. 80 patients are required per arm within the full analysis set. Taking into account that 5% of patients will not qualify for full analysis set, 168 patients should be randomized. If the addition of a reminder app to standard care will result in a significant reduction of radiation toxicity, it could become a helpful tool for these patients.

NCT ID: NCT04110327 Recruiting - Clinical trials for Peripheral Arterial Disease

An All-Comers Observational Study of the MicroStent™ Peripheral Vascular Stent System in Subjects With Peripheral Arterial Disease

HEAL
Start date: October 31, 2019
Phase:
Study type: Observational [Patient Registry]

Non-randomized, multicenter, combined prospective and retrospective cohort analysis consisting of a single arm treated with the MicroStent™ System.

NCT ID: NCT04110067 Recruiting - Myopia Clinical Trials

Clinical Results of Small Incision Lenticule Extraction (SMILE) for the Correction of High Myopia

Start date: January 2016
Phase:
Study type: Observational

Small Incision Lenticule Extraction (SMILE) was introduced in 2011 using the VISUMAX femtosecond laser (Carl Zeiss Meditec, Jena, Germany). It is designed for correction of myopia and myopic astigmatism. It involves the creation of a corneal tissue disk called lenticule and its extraction through a minimally invasive incision, utilizing only a femtosecond laser. This enables rapid visual recovery with very little discomfort to the patient. This observational case series monitors visual and refractive outcomes of myopic correction for more than -7.75 D. It is to - gather long-term results and refractive stability - detect rare complications or side-effects - evaluate the efficacy in a large number of patients

NCT ID: NCT04109833 Recruiting - Clinical trials for Vaccination Reaction

Early Antibiotic Therapy and Vaccination

Start date: September 27, 2019
Phase:
Study type: Observational

Neonatal Sepsis is one of the most common causes of death in preterm infants. Therefore, up to 80% of very low birth weight infants receive antibiotic therapy in their first week of life. Antibiotic therapy is one of the most important influencing factors for the establishment of the intestinal microbiome, which in turn modulates neonatal immune development. In this pilot study, it will be investigated, if antibiotic therapy in the first week of life influences the vaccination response of preterm infants.

NCT ID: NCT04109534 Recruiting - Allergic Asthma Clinical Trials

Effect of a Dietary Fatty Acid Supplementation on Symptoms and Bronchial Inflammation in Patients With Asthma

LCPUFA
Start date: October 1, 2019
Phase: N/A
Study type: Interventional

The proposed study will investigate the effect of a polyunsaturated fatty acid / lipid mixture (LCPUFAs) on the clinical symptoms, bronchial inflammation and lung function in allergic asthma in a bronchial allergen provocation (BAP) model. For this purpose, patients with stable episodic asthma and dust mite allergy will underwent BAP before and after supplementation with LCPUFAs. The clinical symptoms, bronchial inflammation, exhaled NO increase and lung function decline (FEV1) will be analyzed.

NCT ID: NCT04108936 Recruiting - Clinical trials for Peritoneal Carcinomatosis

Longitudinal Study of CRS/HIPEC for Peritoneal Carcinomatoses

CRS/HIPEC
Start date: October 2016
Phase:
Study type: Observational

Longitudinal Study of the Effect of Cytoreductive Surgery and HIPEC in Patients With Peritoneal Carcinomatoses

NCT ID: NCT04107766 Recruiting - Liver Cancer Clinical Trials

NOLA (NeuWave Observational Liver Ablation) Registry

Start date: January 15, 2020
Phase:
Study type: Observational

This is a multicenter, observational registry that follows patients for a total of 5 years from the date of the first liver ablation procedure with the NEUWAVE Microwave Ablation System.

NCT ID: NCT04107376 Recruiting - Adenoma Clinical Trials

Inspection of the Colon Using a Retrograde Viewing Device for Detection of Colorectal Polyps

Start date: December 1, 2018
Phase: N/A
Study type: Interventional

During standard colonoscopy a substantial number of colorectal polyps may be missed. Previous studies have found a 12-28% of miss rate for all polyps, a 31% for hyperplastic polyps and 6-27% for adenomas. In this study it is tested whether a retro viewing endoscope can detect more colorectal polyps in comparisson to standard forward viewing endoscopy. Further, ppolyps detected, mean adenomas per Patient and withdrawal time are recorded.

NCT ID: NCT04106804 Recruiting - Clinical trials for Evaluate Bone Changes in Patients With PsA

Abatacept Bone Effects in Psoriatic Arthritis With Bone Biomarker

Start date: June 6, 2018
Phase: Phase 4
Study type: Interventional

Observation has pointed out, that osteitis present in the MRI scans, predicts bone erosion and that this in accordance with the concept by underlining the importance of bone marrow involvement in arthritis [Krabben A, 2013]. Abatacept with its favourable safety profile preferentially interrupts activation of naïve T cells and perhaps makes the strongest case for exploiting co-stimulatory blockade during the earliest detectable phase of the adaptive immune response at a time when predisposition to autoimmune disease can be detected.

NCT ID: NCT04104607 Recruiting - Clinical trials for Castration-Resistant Prostatic Cancer

the Bispecific PSMAxCD3 Antibody CC-1 in Patients With Castration Resistant Prostate Carcinoma

PSMAxCD3
Start date: November 15, 2019
Phase: Phase 1
Study type: Interventional

This trial is a first in human (FIH) study in patients with castration resistant metastatic prostate cancer (CRPC) after failure of third-line therapy aiming to evaluate safety and efficacy of CC-1, a bispecific antibody (bsAb) with PSMAxCD3 specificity developed within DKTK. CC-1 binds to human prostate-specific membrane antigen (PSMA) on prostate cancer cells as well as to tumor vessels of CRPC, thereby allowing for a dual mode of anti-cancer action. CC-1 was developed in a novel format which not only prolongs serum half-life but most importantly reduces off-target T cell activation with expected fewer side effects. Together with preemptive IL-6 receptor (IL-6R) blockade using tocilizumab, this allows for application of effective bsAb doses with expected high anticancer activity. The study comprises two phases. The first phase is a doseescalation phase with concomitant prophylactic application of tocilizumab to evaluate the maximally tolerated dose (MTD) of CC-1. This is followed by a dose-expansion phase (also with prophylactic IL-6R blockade using tocilizumab), as this approach has been shown to be efficient and beneficial for patients. A translational research program comprising, among others, analysis of CC-1 half-life and the induced immune response as well as molecular profiling in liquid biopsies will serve to better define the mode of action of CC-1 and to identify biomarkers for further clinical development.